LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Third WB diff results from others...

 - UBBFriend: Email this page to someone!    
Author Topic: Third WB diff results from others...
DanielleMC
LymeNet Contributor
Member # 22997

Icon 1 posted      Profile for DanielleMC     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hello
I just got lab results from my 3rd WB done, and it's different from the first two, which confuses me. If a person has Lyme, wouldn't the bands be the same on all tests? Here are my results:
1st WB done July 2009 - IGG - Negative all bands. IGM Positive bands 23 and 41.

2 WB done October 2009 - IGG Positiv bands 41 and 58. IGM positive 23 and 41.

3rd WB done April 2011 - IGG positive band 66. IGM positiv bands 23 and 41.

Why all 3 so different other than the 23 and 41? And CDC requires 5 of 10 IGG to be considered positive. Also, I believe all testing was done by Quest. So confused by all this.

I go see a new LLMD tomorrow. I'm assuming he will have Igenex testing done. Extremely nervous/anxious to the point where I'm making myself sick to my stomach. Anyone else get this anxiety before appointments. I guess I just want it to go away and move on with my life.

--------------------
7/09- WB IGG Neg all bands -WB IGM Pos bands 23 & 41.
Treated w/ 21 days of Doxy.
10/09- WB IGG Pos bands 41 & 58 -WB IGM Pos bands 23 & 41.
04/11- WB IGG Pos band 66 -WB IGM Pos bands 23 & 41 Pos EBV.

Posts: 121 | From Western PA | Registered: Oct 2009  |  IP: Logged | Report this post to a Moderator
Sheryl777
LymeNet Contributor
Member # 17804

Icon 1 posted      Profile for Sheryl777     Send New Private Message       Edit/Delete Post   Reply With Quote 
The CDC criteria of six bands was put in place for vaccines. You can imagine how much confusion and misdiagnoses this has caused.
Posts: 258 | From Spokane, WA | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
Sheryl777
LymeNet Contributor
Member # 17804

Icon 1 posted      Profile for Sheryl777     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sounds like the CDC is now using 5 bands but they were requiring six when I got my test in 2008. My test was also done by Quest and they had the six-band requirement written on the test. What a disservice to us. I had two positive IGGs and my lyme docs had no problem beginning to treat me for lyme.
Posts: 258 | From Spokane, WA | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
little_olive
LymeNet Contributor
Member # 28063

Icon 1 posted      Profile for little_olive     Send New Private Message       Edit/Delete Post   Reply With Quote 
Well, if I understand how a Western Blot works (and I think I do), then no, they wouldn't be the same.

The bands that show up are your body creating antibodies against certain proteins (each band signifies a different protein); these proteins are how the body identifies infections. And the Lyme bacteria are CONSTANTLY changing their proteins, in order to avoid the immune system. So based on which proteins the bacteria are expressing, is which bands will show up. As the bacteria proteins change, so will the positive bands.

Some are almost always there, such as band 41. This band/protein is in the "tail" of the bacteria that they use to get around.

I suspect with IGeneX you'll show a response to band 39, which is probably THE most specific band there is. It only reacts to the DNA of the Lyme bacteria, and does not cross-react like some others.

Your anxiety is probably an additional symptom of the disease, please keep that in mind. It's not just you. Good luck at your appointment and congratulations for taking your health into your own hands!


little olive

--------------------
Myalgic encephalomyelitis, 2002 | Viral onset, following Hep B vaccine
Lyme since '06 | Bartonella since '08 (cured) | Mycoplasma pneumoniae since '08
IGeneX: IgM 31IND 34IND 41+ | IgG 39IND 58+ 41+++
IgG deficiencies and MTHFR 677TT mutations

Posts: 512 | From USA | Registered: Sep 2010  |  IP: Logged | Report this post to a Moderator
little_olive
LymeNet Contributor
Member # 28063

Icon 1 posted      Profile for little_olive     Send New Private Message       Edit/Delete Post   Reply With Quote 
Well if I can find where I got that from I'll come back and show you

Anyway I hope this helps explain why your tests results came out differently each time, Danielle

Posts: 512 | From USA | Registered: Sep 2010  |  IP: Logged | Report this post to a Moderator
annier1071
LymeNet Contributor
Member # 28977

Icon 1 posted      Profile for annier1071     Send New Private Message       Edit/Delete Post   Reply With Quote 
Danielle

You are not crazy. I have severe anxiety still everytime I go to see my LLMD or my GP. I just want all of this to go away too and cause myself to become anxious.

I find that reading too much on all of this (and my llmd has said the same) will cause you to become very fearful of the whole lyme issue. I try to focus on what my LLMD says and only on the positive remarks made on the forum.

I realize that many are very sick on here and I am not well either, but trying to keep my life moving forward (even though I had to stop working for a year so far) is keeping me sane. Just go to the llmd, see what they have to say and if you are not happy with the answer there are always others. Dont overwhelm yourself with all the information you read. You will catch on gradually.

[email protected] contact me anytime Ann

--------------------
Diagnosed with chronic neuro lyme 12/10 after 30 years of vertigo.2 tick bites in 3 yrs from upstate NY. Was on omincef for nine mths..zith and rifampin stopped.Remission~ All the pain and symptoms are back and I am not treating now with biaxin.

Posts: 788 | From New york..queens | Registered: Nov 2010  |  IP: Logged | Report this post to a Moderator
Lymeorsomething
Frequent Contributor (1K+ posts)
Member # 16359

Icon 1 posted      Profile for Lymeorsomething     Send New Private Message       Edit/Delete Post   Reply With Quote 
Well, you're + on all tests so no worries just treat.

No need to run a WB so often. Give treatment a good length of time and then consider a retest.

Running other tests may be more useful (i.e. CD-57, virus panel, bartonella, babs, blood count, ferritin, thyroid, other hormones, etc.)

--------------------
"Whatever can go wrong will go wrong."

Posts: 2062 | From CT | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't waste time or money looking at WB after highly positive in '02. I still have sx, not as severe. I know I'm not dying a slow death today.

I'm still trying to figure out the rest of the story like Paul Harvey would say. Mycoplasma Pn highly ++ in 07 & 09. Doing another test on it soon to see if Rifampin lowered that number in the last year?

Still highly positive with CMV, HHV-6, C-reactive protein. Still trying to find Bart strain, RMSF strain, Rickettsia strain or cousins?

I really think I need to do Bart and some others thru another lab besides LabCorp and Quest.

I've got to attack all the other bad guys. These viruses are no big deal in someone healthy, but when you have an auto-immune illness, lyme and throw these on top...you've got another issue that makes lyme bacteria even harder to get to.

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6478 | From Louisville, Ky | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
DanielleMC
LymeNet Contributor
Member # 22997

Icon 1 posted      Profile for DanielleMC     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you all so very much for your replies. I tend to get lost in all the medical terminology and such of lyme and seem to be more confused aftr researching something thatn I was before. The LLMD also told me the wmore some people read the more they worry themselves. So I am going to just ask questions when I have them to get others points of view and stop reading everything else.

That definitley explains though why my tests are always different. At least one thing is justified... I DO have LD for sure. Now if I can only control this anxiety. It's worse than it's ever been. I worry and freak out about everything. Maybe now that I saw the LLMD, he started me on abx and I'm on the right path, that will all clear up as well.

Again, thanks for your input.

--------------------
7/09- WB IGG Neg all bands -WB IGM Pos bands 23 & 41.
Treated w/ 21 days of Doxy.
10/09- WB IGG Pos bands 41 & 58 -WB IGM Pos bands 23 & 41.
04/11- WB IGG Pos band 66 -WB IGM Pos bands 23 & 41 Pos EBV.

Posts: 121 | From Western PA | Registered: Oct 2009  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.